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Molecule
ID:18665
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₁₃NO₂
Molecular Mass
143.18362
Exact Mass
143.09462866
Charge
0
InChI
InChI=1S/C7H13NO2/c9-7(10)6-8-4-2-1-3-5-8/h1-6H2,(H,9,10)
InChIKey
VRDBIJCCXDEZJN-UHFFFAOYSA-N
Canonic Smiles
OC(=O)CN1CCCCC1
Isomeric Smiles
N1(CC(=O)O)CCCCC1
Calculated Properties
JChem
Acid pKa
1.8857068
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-2.211753
LogD (pH = 7.4)
-2.2123144
Log P
-2.211711
Molar Refractivity
38.2147
Polarizability
14.9515705
Polar Surface Area
40.54
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Properties
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Related Proteins
No Data Available
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
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IUPAC Traditional name
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IUPAC name
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MDL Number
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PubChem SID
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PubChem CID
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Life Chemicals
F1981-0009
Matrix Scientific
020831
ChemBridge
4088006
4401702
Bide Pharmatech
BD28360
A&J Pharmtech
AJA-O13839
AJA-O39802
Academic Data
PubChem
201097
Names and Identifiers
Synonyms
Piperidin-1-yl-acetic acid
piperidin-1-ylacetic acid
1-piperidinylacetic acid
2-(Piperidin-1-yl)acetic acid
IUPAC Traditional name
piperidinoacetic acid
IUPAC name
2-(piperidin-1-yl)acetic acid
Registration numbers
CAS Number
478920-86-4
3235-67-4
14593-04-5
MDL Number
MFCD00461042
PubChem SID
160981972
PubChem CID
201097
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
Product Information
Purity
95+%
Source
96%
Source
98%
Source
Physical Property
0.646
Source
Partition Coefficient